HOW DOES TRANSGENERATIONAL EPIGENETICS CREATE DISEASE VIA POMC?

QUESTION: We have a type 1 diabetic daughter in our home, she is 11 and was diagnosed at 8. Type 1 is where your pancreas stops making insulin, not where you need to eat better, though low carb is a good idea for type 1 as well, so you don't have to pump so much insulin into the body... We go to regular checkups for her with the MD. I know they mean well. But, one of her cholesterol numbers is running high and they want us to reduce saturated fat. They mention the possibility of statin if we can't get the numbers down. NO THANKS. Her HDL and triglycerides are in good shape, but her LDL is high. Will sun exposure help this? Any other ideas?

She was diagnosed at age 8... The doctors just think it was some kind of illness that proceeded it, and that may be. Autoimmune issues also run in the family. I was diagnosed with Juvenile Rheumatoid arthritis at age 12. I was told I'd be in a wheelchair by age 40. Long story, I did some alternative things and was a lot better and lived with mild symptoms until the mid-'30s, kept experimenting, and got even better. Her weight is pretty good... just the LDL is high. But we can do better with carbs with her. In my reading, I have learned that some studies show that all of the vaccinations have something to do with a potential cause. Though we can't point to a timeline in her case, I think there may be something to that too.

ANSWER: Silencing the VDR enhances mitochondrial respiration and this is why obesity, diabetes, and cancer are all linked. What is the link? A lack of sunlight from 290-320nm silences the mitochondrial VDR. Type 1 came from mom transgenerationally having little to no solar exposure and she reprogrammed the egg you became. How do I know? The neuroprotective effect of vitamin D is associated with its influence on neurotrophin in the CNS production and release during POMC neurulation, neuromodulator synthesis, intracellular calcium homeostasis, and prevention of oxidative damage to nervous tissue(DHA protection = elovanoid protection in the egg). Your Mom likely had Neither to get type 1 DM. 

Clinical studies suggest that vit D deficiency may lead to an increased risk of future diseases of the CNS in offspring, particularly schizophrenia, multiple sclerosis, and diabetes. Adequate solar exposure of Mom is critical during pregnancy and for the child in the neonatal period seems to be crucial prevention of these diseases. If Mom never went out pre-pregnancy or during pregnancy, chances are brutally high that the baby never sees the sun either. Neurulation is the job of the thalamus in utero and this is where neurotrophin acts. Vitamin D makes neurotrophin in the CNS in utero. It is loaded with POMC and the VDR so our wide band gap semiconductors create biophotons 290-320 to make melanin and D3 = Vit D deficiency significantly affect brain cell differentiation/proliferation during the neonatal period. 

Since this post is about type 1 diabetes let's review a slide to see how blue light exposure from humans could affect a child who is not even born yet.  Recall in human females, they are born with all their oocytes. So those eggs are heavily programmed by her mother and her grandmother.  Evolution built the system this way so only the best eggs would be selected in new mothers by the leptin melanocortin pathways in the mother that are controlled by POMC.  Yes, Mom, leptin controls fecundity in HUMAN MAMMALS.  

Dad's gametes, called sperm don't show up in his testicles until puberty.  So what Dad's do from puberty to conception is quite important to the future child's construction plan too.  This is codified in methylation patterns and histone modification of chromatin as the video above shows.  So Mom and Dad........how doe slight from your childhoom ultimate effect the beta cells in your future child who isn't even born yet?  Carefully review the slide.  

Blue light or nnEMF exposure via the eye or skin ruin the programming of your clock genes and your skin controls the clock genes in your own gut.  Since women have their eggs fully ready to be programmed at birth this means her light exposure could ruins the clock genes in every egg in her ovary before she has ever thought about sex once in her life.  

Can ladies repiar this problem in their kids post natally when they are young?  

Yes.  If a parent knows they have this risk because a previous birth ended in a jaundiced baby or with a scar from a C section this blog is your wake up call.  Getting very tan and embracing light is key.  If you are a parent who has already made this error your job is to get your young infant/kid out in the sun without any sunscreen.  Yes, I know your flipping out now and your pediatrician is going nuts but they are not the smart tool in the tool box or the following would not be true.  

See the centralized guys do not know what they do not know and when what you do not know turns out to be the most important thing in disease risk...........well this is how unintended consequences happen.  

VIDEO  

Oh, don't think I haven't been warning the masses. they just ignored me because well I am a quack according to the centralized paradigm based in biochemistry understanding supported by Big Pharma.    

1. https://www.linkedin.com/pulse/your-baby-blue-light-jack-kruse/

2. https://www.linkedin.com/pulse/you-entangled-your-kid-via-morning-sickness-jack-kruse/

This is why autism, diabetes, obesity, and mental disease is exploding in our manufactured world that MOTHERS inhabit and they feel the need to be plugged into a grid to live instead of the sun. We've built a prison of poisonous light and the proof is seen in the last 5 generations of kids who are forming the next hominids via regressive evolution.

Big Pharma cannot patent the sun so they hide the truth from the masses of obedient idiots they call customers.

Of course, Big Pharma wants your daughter on a statin. It creates more future revenue streams.

Time to wake up. You’re getting played. That child needs the sun every day all day until diabetes goes away.  Oh, you think this is hyperboles.  Let's look what decentralized medicine data says below.

SUMMARY

You said, "She was diagnosed at age 8... The doctors just think it was some kind of illness that proceeded it, and that may be. Autoimmune issues also run in the family. I was diagnosed with Juvenile Rheumatoid arthritis at age 12. I was told I'd be in a wheelchair by age 40. Long story, I did some alternative things and was a lot better and lived with mild symptoms until the mid-'30s, kept experimenting, and got even better. Her weight is pretty good... just the LDL is high. But we can do better with carbs with her. In my reading, I have learned that some studies show that all of the vaccinations have something to do with a potential cause."  

REPLY: EVERY SINGLE ONE OF THESE FACTORS avove IS a mitochondrial toxin to redox power = REALITY CHECK: why they are all linked to a deep lack of UV light in that family,.......Mommy and Daddy's germ lines had the poison pill in them before the child was even created by your gamete union.  

That union is what created the heteroplasmic egg and voila......we got a type 1 kid.  The childs heteroplasmy rate in the beta cells of the pancreas were already high and that is why the child got diabetic so early in life.  The POMC defect was in her beta cells as soon as you guys got finished having sex.  

  It all fits  How did Mom & Dad screw the pooch initially? 

Vitamin A is linked to all the opsins in the brain as chromophores.    Vitamin D is linked to the skin.    Each Vitamin is entangled with one another because of its connection to the neuroectoderm in the embryo.    If there is a problem in the brain with Vitamin A due to the opsin problem say blue light toxicity or nnEMF exposure no matter if you are naked at the equator you won't make D3 from cholesterol because of this connection. The same connection can be found at the RXR receptor where both act.  That is how transgenerational epigenetics works in humans.  How can parents bad semiconductive like program an egg to create a disease that should not be here, but is now?  

The lipid rafts in humans is dominated by DHA, marine chain fish oil.  No, the answer is not pills.  It is seafood.  It is loaded with electrons that you need to capture sunlight.  Melanin is the photoreceptor in us that CREATES the most electrons in our bodies.  

DHA is the semiconductive fat that is the copper wire in the system but acts like a neurosurgeon when the system is stresed by oxidative damage of any type. 

What does it do?  

Note the photoreceptor destruction issues mentioned in the top line of the slide.  There are hundred of them destroyed besides melanopsin when this occurs in the egg of a women from the time she is born until she gives birth.  Melanin is one of the photoreceptors this slide is referencing with.  This mean a woman who tans regularly before she has choildren is optimizing her future childs life.  

So things that protect photorecepetors are all part of the melanin renovation program for ANY CHILD.  Not surprisingly, docosahexaenoic acid (DHA) is a big help in renovating all photoreceptors in mammals. How?   DHA is broken down into elovanoids under any stressor.  Elovanoids (ELVs) enhance expression of pro-survival proteins in cells undergoing uncompensated oxidative stress.  No other omega 3 has this ability.  This is why evolution has not replaced it once in 650 million years of evolutionary history on EARTH.  Let that sink in.  DHA helps stimulate autophagy to recycle photoreceptors in mammals.  We have the most DHA in our tissues as a mammal for a reason; our brain is unique in the mammalian family.  DHA also fills the human oocyte.  

Oh.........Happy Mother's Day.  

I hope all you Mother's realize how we work and why kids are the way they are.  Because we programmed their egg with our decisions around light.  Change that before you decide to become a parent.  It will save a lot of heartache.  

CITES: 

My cerebral cortex